Slamanig Stefan, Lemus Nicholas, Lai Tsoi Ying, Singh Gagandeep, Mishra Mitali, Abdeljawad Adam, Boza Marta, Dolange Victoria, Singh Gagandeep, Lee Benhur, González-Domínguez Irene, Schotsaert Michael, Krammer Florian, Palese Peter, Sun Weina
Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA; Swammerdam Institute for Life Sciences, University of Amsterdam, Amsterdam, the Netherlands.
Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Vaccine. 2025 Jan 25;45:126586. doi: 10.1016/j.vaccine.2024.126586. Epub 2024 Dec 12.
The rapid development of coronavirus disease 2019 (COVID-19) vaccines has helped mitigate the initial impact of the pandemic. However, in order to reduce transmission rates and protect more vulnerable and immunocompromised individuals unable to mount an effective immune response, development of a next-generation of mucosal vaccines is necessary. Here, we developed an intranasal Newcastle disease virus (NDV)-based vaccine expressing the spike of the XBB.1.5 variant stabilized in its pre-fusion conformation (NDV-HXP-S). We demonstrated that one or two intranasal immunizations with live NDV-HXP-S expressing the XBB.1.5 spike induces systemic and mucosal antibody responses in mice and protects them from a challenge with the XBB.1.5 variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Furthermore, one or two intranasal vaccinations with NDV-HXP-S XBB.1.5 protected hamsters from variant matched infection and reduced virus emission, thereby providing complete protection to naïve animals in a direct contact transmission study. The data shown in this study supports the notion that intranasal vaccination with variant-adapted NDV-HXP-S induces protective mucosal immunity and reduces transmission rates, highlighting the robust protective efficacy of a single mucosal vaccination in mice and hamsters.
2019冠状病毒病(COVID-19)疫苗的迅速发展有助于减轻大流行的初步影响。然而,为了降低传播率并保护更多无法产生有效免疫反应的脆弱和免疫功能低下个体,开发下一代黏膜疫苗是必要的。在此,我们开发了一种基于鼻内接种新城疫病毒(NDV)的疫苗,该疫苗表达处于融合前构象稳定的XBB.1.5变体的刺突蛋白(NDV-HXP-S)。我们证明,用表达XBB.1.5刺突蛋白的活NDV-HXP-S进行一次或两次鼻内免疫可在小鼠体内诱导全身和黏膜抗体反应,并保护它们免受严重急性呼吸综合征冠状病毒2(SARS-CoV-2)XBB.1.5变体的攻击。此外,用NDV-HXP-S XBB.1.5进行一次或两次鼻内接种可保护仓鼠免受变体匹配感染并减少病毒排放,从而在直接接触传播研究中为未感染动物提供完全保护。本研究所示数据支持以下观点,即使用适应变体的NDV-HXP-S进行鼻内接种可诱导保护性黏膜免疫并降低传播率,突出了单次黏膜接种在小鼠和仓鼠中的强大保护效力。